US5795954A - Factor VIIa inhibitors from Kunitz domain proteins - Google Patents

Factor VIIa inhibitors from Kunitz domain proteins Download PDF

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US5795954A
US5795954A US08/206,310 US20631094A US5795954A US 5795954 A US5795954 A US 5795954A US 20631094 A US20631094 A US 20631094A US 5795954 A US5795954 A US 5795954A
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xaa
cys
gly
phe
ala
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Robert A. Lazarus
Mark S. Dennis
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Genentech Inc
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Genentech Inc
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Assigned to GENENTECH, INC. reassignment GENENTECH, INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: DENNIS, MARK S., LAZARUS, ROBERT A.
Priority to US08/399,115 priority patent/US5880256A/en
Priority to PCT/US1995/002637 priority patent/WO1995023860A2/fr
Priority to JP7523045A priority patent/JPH09509838A/ja
Priority to US08/398,010 priority patent/US5834244A/en
Priority to MX9603775A priority patent/MX9603775A/es
Priority to EP95913532A priority patent/EP0748380A1/fr
Priority to CA002184058A priority patent/CA2184058A1/fr
Priority to US08/398,628 priority patent/US5863893A/en
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/81—Protease inhibitors
    • C07K14/8107—Endopeptidase (E.C. 3.4.21-99) inhibitors
    • C07K14/811—Serine protease (E.C. 3.4.21) inhibitors
    • C07K14/8114—Kunitz type inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Definitions

  • This invention relates to novel Kunitz domain proteins having tissue factor•Factor VIIa inhibiting activity, DNA encoding these proteins, and recombinant materials and methods for producing these Factor VIIa inhibitors.
  • the invention further relates to pharmaceutical compositions containing Factor VIIa inhibitors for treatment of diseases where inhibition of Factor VIIa, Factor XIa, plasma kallikrein, and plasmin is indicated.
  • thrombosis accounts for about 40% of the deaths in the United States.
  • Current treatments for thrombotic disorders involve the use of anticoagulant drugs (e.g., heparin, coumadin) that have non-specific mechanisms of action. These drugs can cause bleeding thus limiting their use.
  • tissue factor•Factor VIIa complex (TF•FVIIa) is a primary initiator of blood coagulation (Carson, S. D. and Brozna, J. P., Blood Coag. Fibrinol. 4: 281-292 1993!; Davie, E. W. et al., Biochemistry 30: 10363-10370 1991!; Rapaport, S. I. and L. V. M. Rao, Arterioscler. Thromb. 12: 1111-1121 1992! (see FIG. 1).
  • FVIIa Factor VIIa
  • FVIIa Factor VIIa
  • zymogen Factor VIIa FVII
  • Tissue factor contains 263 residues and is an integral membrane cofactor that is expressed constitutively in cells separated from plasma by the vascular endothelium (Carson, S. D. and J. P. Brozna, Blood Coag Fibrinol 4: 281-292 1993!).
  • vascular endothelium Carson, S. D. and J. P. Brozna, Blood Coag Fibrinol 4: 281-292 1993!.
  • Factor XIIa has also been implicated in the activation of FVII.
  • the TF•FVIIa complex initiates the extrinsic pathway of the coagulation cascade by activation of Factor X (FX) to Factor Xa (FXa) , Factor IX (FIX) to Factor IXa (FIXa), and additional FVII to FVIIa.
  • FX Factor X
  • FXa Factor Xa
  • FIX Factor IX
  • FIXa Factor IXa
  • FVIIa Factor IXa
  • TF•FVIIa tissue factor pathway inhibitor
  • TFPI tissue factor pathway inhibitor
  • LACI lipoprotein associated coagulation inhibitor
  • EPI lipoprotein associated coagulation inhibitor
  • TFPI contains an acidic amino terminal region followed by three Kunitz-type domains and a basic carboxy terminal region.
  • TFPI is thought to inhibit TF•FVIIa in a FXa dependent manner, first binding FXa via the second Kunitz domain followed by binding FVIIa via the first Kunitz domain (Girard, T. J. et al., Nature 338: 518-520 1989!).
  • TFPI is a poor inhibitor of the TF•FVIIa complex (Girard, T. J. et al., Science 248: 1421-1424 1990!).
  • serpin antithrombin III AT III
  • has also been shown to inhibit TF•FVIIa activity in the presence of heparin (Rao, L. V. M.
  • TFPI variants of TFPI have been made that also inhibit TF•FVIIa activity.
  • a variant that contains the first two Kunitz domains has been made and characterized (Hamamoto et al. J. Biol. Chem. 268: 8704-8710 1993!; Petersen et al. J. Biol. Chem. 268: 13344-13351 1993!).
  • TFPI and variants have been shown to affect hemostasis in animal models of arterial reocclusion after thrombolysis (Haskel, E. J. et al., Circulation 84: 821-827 1991!), venous thrombosis (Holst, J.
  • TFPI may not have all of the properties desired for an anticoagulant agent for the treatment of thrombotic disease.
  • the dependence of FXa inhibition by TFPI prior to the inhibition of TF•FVIIa may have undesirable effects.
  • FXa is produced by both the intrinsic and extrinsic pathways
  • inhibition of FXa may totally inhibit coagulation and lead to undesirable side effects such as bleeding; a selective inhibitor of the extrinsic or intrinsic pathways may not lead to this problem.
  • heparin may affect the activity of TFPI.
  • the carboxyl terminus of TFPI may be required for maximal activity (Wesselschmidt, R. et al., Blood 79:2004-2010 1992!; Nordfang, O.
  • TFPI is cleaved by human leukocyte elastase between the first two Kunitz domains which results in the loss of TF•FVIIa inhibitory activity (Higuchi, D. A. et al., Blood 79: 1712-1719 1992!).
  • Bovine pancreatic trypsin inhibitor also referred to as aprotinin
  • K i 30 ⁇ M
  • BPTI has recently been shown to inhibit TF-induced coagulation; however, ca. 75 ⁇ M was needed to prolong the clotting time 1.4-fold in a PT assay (van den Besselaar, A. M. H. P. et al., Thromb Haemostas 69: 298-299 1993!).
  • Factor XIa is a glycosylated serine protease produced in blood from its zymogen, Factor XI (FXI). It is composed of a homodimer of two identical disulfide-linked proteins each having a molecular weight of 80,000 Da (Kitchens, C. S., Semin. Thromb. Hemostas. 17: 55-72 1991!). In blood, most of the protein circulates bound to high molecular weight kininogen (HMWK). FXI is normally present at a concentration of ca. 4.5 ⁇ g/ml.
  • FXIIa can be activated by a number of serine proteases; FXIIa is thought to be a major activator, although thrombin has also recently been implicated (Galiani, D. and Broze Jr., G. J., Science 253: 909-912 1991!).
  • FXIIa can activate prekallikrein to kallikrein and FXI to FXIa; the kallikrein formed can activate more Factor XII to FXIIa.
  • FXIa activates FIX to FIXa, which in the presence of Factor VIII leads to the formation of FXa and ultimately a fibrin clot (see FIG. 1).
  • Serpin ⁇ 1-antitrypsin also known as ⁇ 1-proteinase inhibitor
  • Serpins serine protease inhibitors
  • Serpins serine protease inhibitors
  • ⁇ 1 -proteinase inhibitor have been well characterized for their ability to inhibit various proteases because of their therapeutic potential to control proteolysis in thrombosis, shock, and inflammation (Schapira, M. et al., Trends Cardiovasc. Med., 4:146-151 1991!; Patston, P. A. et al., J. Biol. Chem.
  • FXIa Another inhibitor of FXIa is protease nexin-2, the secreted form of the Alzheimer's amyloid ⁇ -protein precursor, sometimes referred to as A ⁇ PP 751 and A ⁇ PP 770 for the different isoforms of this protein (Van Nostrand, W. E. et al., J. Biol. Chem. 265: 9591-9594 1990!; Wagner, S. L. et al., Biochem. Biophys. Res. Commun. 186: 1138-1145 1992!; Smith, R. P. et al, Science 248: 1126-1128 1990!).
  • This protein contains a Kunitz domain which has been designated KPI (61 residues)(Wagner, S. L. et al., Biochem.
  • Prekallikrein is a glycoprotein comprised of a single polypeptide chain with a molecular weight of 80,000 Da and is present in normal plasma at a concentration of ca. 50 ⁇ g/ml (600 nM). In blood, 75% of prekallikrein circulates bound to HMWK. It is a serine protease zymogen which can be activated by FXIIa (see FIG. 1). Kallikrein consists of 2 disulfide bonded chains of 43,000 and 33,000-36,000 Da. The light chain of kallikrein contains the enzymatic domain while the heavy chain appears to be required for surface dependent activation of coagulation.
  • Kallikrein cleaves HMWK to form bradykinin (a potent vasodilator and endothelial cell activator), can activate prourokinase and plasminogen (fibrinolytic), and feeds back for reciprocal activation of surface bound FXII to FXIIa (see FIG. 1). In addition it can also stimulate neutrophils causing the release of elastase. Both Factor XIIa and kallikrein can lead to plasmin generation causing fibrinolysis.
  • the major physiological inhibitor of kallikrein is the serpin C1 inhibitor, which inhibits irreversibly.
  • HMWK has been shown to protect kallikrein from inhibition by C1 inhibitor although both proteins bind to kallikrein at different sites.
  • ⁇ 2-macroglobulin is another major inhibitor of kallikrein.
  • Antithrombin-III can also inhibit kallikrein, but slowly even in the presence of heparin.
  • ⁇ 2-antiplasmin and ⁇ 1-antitrypsin are poor inhibitors of kallikrein.
  • a mutant form of ⁇ 1 -proteinase inhibitor ⁇ 1 -proteinase inhibitor-Pittsburgh) that contains an Arg in the P 1 position and an Ala in the P 2 position has been shown to be a more potent inhibitor of Factor XIIf (FXIIf) and kallikrein compared to C1 inhibitor, the most potent known natural inhibitor of these proteases (Schapira, M. et al., J. Clin. Invest 80:582-585 1987!; Patston, P. A. et al., J. Biol. Chem. 265:10786-10791 1990!). Rats treated with this mutant were partially protected from the hypotension resulting from injection of FXIIf.
  • FXIIf Factor XIIf
  • BPTI Basic pancreatic trypsin inhibitor
  • aprotinin Basic pancreatic trypsin inhibitor
  • a variant of BPTI having arginine at position 15 has been made semisynthetically and found to inhibit plasma kallikrein with a Ki of 15 nM, about 20-fold higher affinity than BPTI (Scott, C. F. et al., Blood 69: 1431-1436 1987!).
  • BPTI has been used to treat patients with acute pancreatitis (Fritz, H. and Wunderer, G., Arzneim.-Forsch. Drug Res.
  • soybean trypsin inhibitor has been shown to inhibit bradykinin formation and the initial hypotension induced by endotoxin in rats (Katori, M. et al., Br. J. Pharmacol. 98:1383-1391 1989!).
  • TF is found on the surface of the endothelium as well as monocytes and may become activated during the inflammatory response (Altieri, D. A., Blood 81: 569-579 1993!).
  • inhibitors of the TF•FVIIa complex may be useful as anticoagulants and as antiinflammatory agents.
  • a monoclonal antibody to TF has been shown to prevent mortality in a baboon model of septic shock (Taylor Jr., F. B. et al., Circ. Shock 33:127-134 1991!).
  • a TF antibody has also shown that TF may play a role in focal cerebral ischemia (Thomas, W. S. et al., Stroke 24: 847-854 1993!).
  • a monoclonal antibody against rabbit TF inhibited thrombus formation in carotid arteries (Pawashe, A. B. et al., Circ. Res. 74: 56-63 1994!).
  • Contact activation is a surface mediated pathway responsible in part for the regulation of inflammation and thrombosis as mediated by coagulation, kinin, fibrinolysis, complement, and other relevant pathways (see FIG. 1).
  • the proteins involved in this pathway include FXII (Hageman Factor), prekallikrein (Fletcher Factor), FXI, high molecular weight kininogen (HMWK), and C1 inhibitor (DeLa Cadena, R. A., et al. in Hemostasis and Thrombosis: Basic Principles and Clinical Practice (Colman, R. W., Hirsh, J., Marder, V., & Salzman, E. W., eds.) pp. 219-240, J.
  • Septic shock is the most common cause of death of humans in intensive care units in the United States (Parillo, J. E. et al., Ann. Int. Med. 113:227-242 1990!; Schmeichel C. J. and McCormick D., BioTechnol. 10:264-267 1992!). It is usually initiated by a local nidus of infection that invades the blood stream. Incidences of sepsis and shock can arise from infections with either gram negative, gram positive bacterial or fungal microorganisms. All these organisms seem to induce a common pattern of cardiovascular dysfunction. In recent years aggressive fluid infusion therapy has been accepted as a primary means of treatment for septic shock.
  • Adequate repletion of fluid is associated with an elevated cardiac output and low vascular resistance.
  • septic shock results in a severe decrease in systemic vascular resistance and generalized blood flow maldistribution. Aggressive therapy reverses shock and death in about 50% of the cases. Unresponsive hypotension resulting from a very low vascular resistance cannot be corrected by fluid infusion.
  • approximately 75% die from persistent hypotension and the remainder due to multiple organ system failure (see FIG. 1).
  • the contact system can participate in the generation of many vasoactive mediators such as bradykinin, FXIIa, FXIIf and C5a, which are thought to play a role in the pathogenesis of fatal shock.
  • Bradykinin, FXIIa, and FXIIf are potent inducers of hypotension while C5a is an inducer of vasodilation and vasopermeability.
  • the levels of FXII, prekallikrein, and high molecular weight kininogen are decreased significantly during non-fatal shock, but are most severely depressed during fatal septic shock to approximately 30%, 57% and 27% of normal values respectively. These changes are noted regardless of whether the septic state is caused by gram positive or gram negative bacteria.
  • the contact activation pathway is also involved in both fibrin deposition and lysis, as well as triggering neutrophil activation, activation of complement and modulation of blood pressure.
  • ARDS is a complex pulmonary disorder affecting 150,000 people in the U.S. yearly with a 50% mortality rate.
  • Leukocytes, platelets and the proteolytic pathways of coagulation and complement mediate ARDS.
  • ARDS involves activation of the contact activation pathway and depletion of C1 inhibitor.
  • Sepsis induced ARDS results in more severe DIC and fibrinolysis, more fibrin degradation products and reduced ATIII levels compared to trauma induced ARDS (Carvalho, A. C. et al., J. Lab. Clin. Med. 112:270-277 1988!).
  • DIC Disseminated intravascular coagulation
  • cytokine antagonists to endotoxin, tissue factor, tumor necrosis factor (TNF), neutrophils, etc.
  • kinin antagonists to endotoxin, tissue factor, tumor necrosis factor (TNF), neutrophils, etc.
  • kinin antagonists to endotoxin, tissue factor, tumor necrosis factor (TNF), neutrophils, etc.
  • bactericidal permeability increasing protein PAF antagonists
  • C1 inhibitor C1 inhibitor
  • DEGR-FXa activated protein C
  • the Kunitz-type protease inhibitor domains found in TFPI are found among other mammalian proteins including BPTI, Alzheimer's amyloid ⁇ -protein precursor, and inter- ⁇ -trypsin inhibitor (Creighton, T. E. and I. G. Charles, Cold Spring Harbor Symp. Quant. Biol. 52: 511-519 1987!; Salvesen, G. and Pizzo, S., in Hemostasis and Thrombosis: Basic Principles and Clinical Practice (Colman, R. W., Hirsh, J., Marder, V., & Salzman, E. W., eds.) pp. 241-258, J. B. Lippincott Co., Philadelphia 1994! (FIG. 2).
  • Kunitz-type protease inhibitors have also been prepared from the ⁇ -3 chain of human type VI collagen (see WO 93/14119). They have also been identified in many snake venoms. Recently, Kunitz inhibitors of TF•FVIIa have been prepared from BPTI using phage display technology (De Maeyer et al., Thrombosis and Haemostasis Abstracts, XIV th Congress of the International Society on Thrombosis and Haemostasis, p 888 Ab. No. 1245 1993!). These authors report a mutant BPTI (T11D, K15R, R17L, I18H, I19L, V34Y, R39L and K46E) having a K i for TF•FVIIa of 0.5 nM.
  • Kunitz domains are generally stable proteins containing about 60 residues and six specifically spaced cysteines that are present in disulfide bonds. They are known to be slow, tight-binding, reversible inhibitors of serine proteases that bind to the active site and inhibit according to the standard mechanism. Subsequent cleavage between the P 1 and P 1 ' residues occurs very slowly if at all (Bode, W. and Huber, R., Eur. J. Biochem. 204: 433-451 1992!; Laskowski, M., Jr. and Kato, I., Annu. Rev. Biochem. 49: 593-626 1980!).
  • either Arg or Lys is generally preferred.
  • methionine is sometimes found at the P1 position and may also be preferable for good inhibition of serine proteases (McGrath, M. E. et al., J. Biol. Chem. 266:6620-6625 1991!).
  • the introduction of residues such as Val, Leu, or Ile at the P 1 position of Kunitz domains leads to potent inhibitors of human leukocyte elastase (HLE) and concomitant loss of the wild type inhibitory activity (Beckmann, J. et al., Eur. J. Biochem. 176: 675-682 1988!; Sinha, S. et al., J. Biol. Chem.
  • Positions 11, 15, 17, and 19 are relatively variable among Kunitz domains (Creighton, T. E. and I. G. Charles, Cold Spring Harbor Symp. Quant. Biol. 52: 511-519 1987!).
  • Position 13 is normally a Pro; however, other residues are sometimes found here.
  • Position 12 is almost always a Gly.
  • substitution of other residues for Pro and vice versa might also lead to conformational changes in the main chain which could affect binding.
  • the cysteine residues at positions 14 and 38 that form a disulfide bond are always found in Kunitz domains; however other residues such as Ala, Gly, Ser, or Thr may substitute for the cysteines (Marks, C. B. et al., Science, 235: 1370-1373 1987!).
  • residues 13 and 39 as well as residues 17 and 34 are in close proximity (FIG. 3) (Hynes, T. R. et al., Biochemistry 29: 10018-10022 1990!). Therefore, the potential interactions of residues 34 and 39 with the primary binding loop of APPI were investigated to address whether these positions would affect binding. Residues at positions 16 and 18 are generally more invariant among Kunitz domains (Creighton, T. E. and I. G. Charles, Cold Spring Harbor Symp. Quant. Biol. 52: 511-519 1987!); however, different residues at these positions may also alter binding.
  • residues at positions 11 through 19, 34, 38, and 39 may all affect the binding affinity and specificity towards serine proteases (FIG. 3). Other residues may be of importance as well.
  • APPI and BPTI have a methionine at position 52, although other Kunitz domains have a variety of residues at this position.
  • Methionine at this position can be replaced by different residues which may be beneficial with respect to producing the protein. For example, methionine is susceptible to oxidation to form methionine sulfoxide, which can complicate purification.
  • protein can be made recombinantly as a fusion protein, followed by cleavage with CNBr, which cleaves at methionine residues (Auerswald, E. A.
  • the 61 residue Kunitz protease inhibitor domain of the Alzheimer's amyloid ⁇ -protein precursor (KPI), binds to the active site of mammalian serine proteases trypsin, chymotrypsin and Factor XIa with high affinity (Wagner, S. L. et al., Biochem. Biophys. Res. Commun. 186: 1138-1145 1992!). Similar results were found with a fusion protein containing this domain (Sinha, S. et al., J. Biol. Chem. 266: 21011-21013 1991!).
  • the KPI domain has also been shown to inhibit FIXa activity, although much less potently than protease nexin-2, from which it was derived (Schmaier A. H. et al., J. Clin. Invest. 92: 2540-2545 1993!).
  • the KPI domain at 100 ⁇ M independently inhibited the coagulant activity of both Factor Xa and VIIa in plasma more than twofold over control.
  • this inhibition was at least two orders of magnitude weaker than the inhibition of Factor XIa by the KPI domain, which at ⁇ 0.5 ⁇ M resulted in a twofold prolongation of the Factor XIa coagulant assay.
  • APPI as a scaffold since (a) it has been readily expressed in bacteria such as E.
  • potent serine protease inhibitors that reversibly inhibit proteases of the coagulation, contact activation, fibrinolysis, inflammation, complement activation, and hypotensive pathways for the treatment of diseases that are affected by these pathways. It is further an object of this invention to provide potent inhibitors capable of inhibiting Factor VIIa, Factor XIa, kalkallikrein, and plasmin. Additionally, it is an object to provide synthetic methods for producing these inhibitors for therapeutic intervention.
  • composition of matter capable of inhibiting a serine protease selected from Factor VIIa, Factor XIa, plasma kallikrein, and plasmin, comprising a purified polypeptide having an amino acid sequence represented by Structural Formula I:
  • R 1 represents a peptide comprising from 5 to 250 naturally occurring amino acid residues wherein at least one residue is Cys;
  • R 2 represents a peptide having 14 amino acid residues wherein at least one residue is Cys
  • R 3 represents a tripeptide
  • R 4 represents a peptide comprising from 12 to 250 amino acid residues wherein at least one residue is Cys;
  • Xaa 11 is a naturally occurring amino acid residue selected from the group Pro, Arg, Ala, Glu, Gly, and Thr;
  • Xaa 12 represents Gly
  • Xaa 13 is a naturally occurring amino acid residue selected from the group Pro, Leu, Trp, Val, Gly, Phe, His, Tyr, Ala, Ile, Glu, and Gln;
  • Xaa 14 is a naturally occurring amino acid residue selected from Cys, Ala, Ser, Thr, and Gly;
  • Xaa 15 is a naturally occurring amino acid residue selected from Met, Arg, and Lys;
  • Xaa 16 is a naturally occurring amino acid residue selected from Gly and Ala;
  • Xaa 17 is a naturally occurring amino acid residue selected from the group Met, Leu, Ile, Arg, Tyr, and Ser;
  • Xaa 18 is a naturally occurring amino acid residue selected from the group Ile, His, Leu, Met, Tyr, and Phe;
  • Xaa 19 is a naturally occurring amino acid residue selected from the group Leu, Arg, Ala, Lys, and Ile;
  • Xaa 34 is a naturally occurring amino acid residue selected from the group Phe, Ile, Ser, Leu, Tyr, Trp, and Val;
  • Xaa 38 is a naturally occurring amino acid residue selected from Cys, Ala, Ser, Thr, and Gly;
  • Xaa 39 is a naturally occurring amino acid residue selected from the group Tyr, Gly, Trp, His, and Phe; provided
  • R 1 is not Xaa 1 -Asp-Ile-Cys-Lys-Pro-Lys-Asp (SEQ ID NO: 1) where Xaa 1 is His or 1-5 amino acid residues; and
  • a preferred polypeptide represented by Formula I has an apparent dissociation constant (K i *) with respect to Tissue Factor•Factor VIIa of less than about 100 nM, more preferably less than 10 nM and most preferably 3 nM or lower.
  • the preferred polypeptide also has an apparent dissociation constant (K i *) with respect to both Factor XIa and kallikrein of less than about 10 nM and most preferably 2 nM or lower.
  • Polypeptides of Formula I that are potent inhibitors of all three of; TF•FVIIa, FXIa, and kallikrein preferably have Xaa 18 -Xaa 19 as Ile-Leu.
  • the preferred polypeptide specifically inhibits TF•FVIIa and has an apparent dissociation constant (K i *) with respect to both Factor XIa and kallikrein of greater than about 50 nM and most preferably greater than about 80 nM.
  • Polypeptides of Formula I that are specific potent inhibitors of TF•FVIIa preferably have Xaa 18 -Xaa 19 as Met-Lys/Arg.
  • the preferred polypeptide represented by Structural Formula I comprises about 58 amino acid residues in which R 1 is a 10 residue peptide, R 2 is a 14 residue peptide, R 3 is a tripeptide, and R 4 is a 19 residue peptide, and where residue 5, 14, 30, 38, 51 and 55 are Cys. Also preferably, residues 12 and 37 are Gly, residues 33 and 45 are Phe, residue 35 is Tyr, and residue 43 is Asn.
  • Exemplary preferred polypeptides of Structural Formula I are as follows:
  • R 1 is selected from the group
  • R 2 is selected from the group
  • R 3 is selected from the group
  • R 4 is selected from the group
  • Xaa 11 is Pro
  • Xaa 12 is Gly
  • Xaa 13 is selected from the group Pro, Val, Leu, and Trp;
  • Xaa 14 is Cys
  • Xaa 15 is Arg or Lys
  • Xaa 16 is Ala
  • Xaa 17 is Met or Leu
  • Xaa 18 is Met or Ile
  • Xaa 19 is Leu, Lys or Arg
  • Xaa 34 is Phe, Val, Ile, or Tyr;
  • Xaa 38 is Cys
  • Xaa 39 is Tyr, Gly, or His.
  • the present invention encompasses a composition of matter comprising isolated nucleic acid, preferably DNA, encoding the protein component of a composition of matter comprising a polypeptide represented by Structural Formula I.
  • the invention further comprises an expression control sequence operably linked to the DNA molecule, an expression vector, preferably a plasmid, comprising the DNA molecule, where the control sequence is recognized by a host cell transformed with the vector, and a host cell transformed with the vector.
  • Preferred expression vectors of the present invention may be selected from; pBR322, phGH1, pBO475, pRIT5, pRIT2T, pKK233-2, pDR540, and pPL-lambda, with the most preferred vector being pSAlz1.
  • Preferred host cells containing the expression vector of the present invention may be selected from E. coli K12 strain 294 (ATCC No. 31446), E. coli strain JM101, E. coli B, E. coli X1776 (ATCC No. 31537), E. coli c600, E. coli W3110 (F-, gamma-, prototrophic, ATCC No. 27325), Bacillus subtilis, Salmonella typhimurium, Serratia marcesans, and Pseudomonas species, with the most preferred host cell being E. coli W3110 (ATCC No. 27325), or a derivative thereof such as the protease deficient strain 27C7.
  • composition of the present invention may be made by a process which includes the steps of isolating or synthesizing nucleic acid sequences encoding any of the amino acid sequences described above, ligating the nucleic acid sequence into a suitable expression vector capable of expressing the nucleic acid sequence in a suitable host, transforming the host with the expression vector into which the nucleic acid sequence has been ligated, culturing the host under conditions suitable for expression of the nucleic acid sequence, whereby the protein encoded by the selected nucleic acid sequence is expressed by the host.
  • the ligating step may further contemplate ligating the nucleic acid into a suitable expression vector such that the nucleic acid is operably linked to a suitable secretory signal, whereby the amino acid sequence is secreted by the host.
  • the secretory signal may be selected from the group consisting of the leader sequence of stIl, lamB, herpes gD, lpp, alkaline phosphatase, invertase, and alpha factor and is preferably stII.
  • the present invention further extends to therapeutic applications for the compositions described herein.
  • the invention includes a pharmaceutical composition comprising a pharmaceutically acceptable excipient and a purified amino acid sequence represented by Formula I.
  • Those applications include, for example, a method for inhibiting thrombus formation in a mammal comprising administering a pharmaceutically effective amount of the pharmaceutical composition to the mammal.
  • the pharmaceutically effective amount may be between about 0.001 nM and 1.0 mM, is preferably between about 0.1 nM and 100 82 M, and is most preferably between about 1.0 nM and 50 ⁇ M.
  • the pharmaceutical composition may be administered prior to, following, or simultaneously with administration of a fibrinolytic or thrombolytic agent such as tissue plasminogen activator, streptokinase, urokinase, prourokinase, and modifications thereof.
  • the pharmaceutical composition may be administered in combination with an anticoagulant.
  • other applications include, for example, a method of treating a mammal for which inhibiting Factor VIIa, Factor XIa, plasma kallikrein, or plasmin is indicated comprising administering a pharmaceutically effective amount of the pharmaceutical composition to the mammal.
  • indications include; inflammation, septic shock, hypotension, ARDS, DIC, cardiopulmonary bypass surgery, and bleeding from postoperative surgery.
  • FIG. 1 Schematic outline of selected enzymes and mediators that modulate the coagulation, contact, fibrinolytic, inflammatory, and complement pathways. Activation of these pathways can lead to the clinical states indicated.
  • FIG. 2 Sequence alignment of Kunitz domains from mammalian sources. Aligned are TF7I-C (residues 1-58) (SEQ ID NO: 33), which is described herein; APPI (residues 1-58) (SEQ ID NO: 54) from human Alzheimer's disease amyloid ⁇ -protein precursor, residues 287-344 (Castro, M. et al. FEBS Lett.
  • TFPI-KD1 (residues 22-79) (SEQ ID NO: 35), TFPI-KD2 (residues 93-150) (SEQ ID NO: 36), and TFPI-KD3 (residues 185-242) (SEQ ID NO: 37) of human TFPI, respectively (Broze Jr., G. J. et al., Biochemistry 29: 7539-7546 1990!); ITI-KD1 and ITI-KD2, (residues 22-79 and 78-135) (SEQ ID NO: 38 and 39) of human inter- ⁇ -trypsin inhibitor, respectively (Vetr, H.
  • FIG. 3 Model of APPI and other Kunitz domains.
  • the numbers refer to the residues found in APPI and other Kunitz domains; residue 15 corresponds to the P 1 residue.
  • the shaded area refers to the primary (residues 11-19) and secondary (residues 34-39) binding loops of APPI and other Kunitz domains.
  • FIG. 4 Sequence and Apparent Equilibrium Dissociation Constants for Kunitz Domain Variants. Amino acids positions corresponding to those in APPI are indicated.
  • FIG. 5 Determination of the Apparent Equilibrium Dissociation Constants of TF7I-C and APPI with TF•FVIIa.
  • the inhibitory activity is expressed as the fractional activity (inhibited rate/uninhibited rate) at varying inhibitor concentrations.
  • the FVIIa and TF 1-243 concentrations were 10 nM and 50 nM, respectively.
  • the apparent equilibrium dissociation constants were determined by nonlinear regression analysis of the data using equation 1 and yielded K i * values of 2.1 nM for TF7I-C ( ⁇ ) and 300 nM for APPI ( ⁇ ).
  • the lines represent best fits of the data to equation 1 for the calculated K i *.
  • the data is representative of nine independent determinations for TF7I-C and seven for APPI.
  • the fractional activity for 1:1 stoichiometric inhibition is represented by a dashed line.
  • FIG. 6 Prolongation of clotting time in the PT assay in normal human plasma.
  • concentration of TF7I-C ( ⁇ ) and APPI ( ⁇ ) are plotted vs. the fold prolongation of clotting time upon initiation by TF membranes.
  • the uninhibited clotting time was 48 sec.
  • FIG. 7 Prolongation of clotting time in the APTT assay in normal human plasma.
  • the concentration of TF7I-C ( ⁇ ) and APPI ( ⁇ ) are plotted vs. the fold prolongation of clotting time upon initiation by ellagic acid.
  • the uninhibited clotting time was 31 sec.
  • amino acid or amino acid residue refers to naturally-occurring L ⁇ -amino acids or residues, unless otherwise specifically indicated.
  • the commonly used one- and three-letter abbreviations for amino acids are use herein (Lehninger, A. L., Biochemistry, 2d ed., pp. 71-92, Worth Publishers, New York 1975!).
  • mutants or variants When referring to mutants or variants, the wild type amino acid residue is followed by the residue number and the new or substituted amino acid residue. For example, substitution of Pro for wild type Thr in residue position 11 is denominated Thr11Pro.
  • the P 1 residue refers to the position proceeding the scissile peptide bond of the substrate or inhibitor as defined by Schechter and Berger (Schechter, I. and Berger, A., Biochem. Biophys. Res. Commun. 27: 157-162 1967!).
  • “Expression vector” refers to a DNA construct containing a DNA sequence which is operably linked to a suitable control sequence capable of effecting the expression of the protein encoded by the DNA in a suitable host.
  • control sequences generally include a promoter to effect transcription, an optional operator sequence to control transcription, a sequence encoding suitable mRNA ribosome binding sites, and sequences which control termination of transcription and translation.
  • the vector may be a plasmid, a phage particle or "phagemid", or simply a potential genomic insert.
  • the vector may replicate and function independently of the host genome, or may, in some instances, integrate into the genome itself.
  • plasmid "vector” and “phagemid” are sometimes used interchangeably as the plasmid is the most commonly used form of vector at present.
  • the invention is intended to include such other forms of expression vectors which serve equivalent functions and which are, or which become, known in the art.
  • operably linked when describing the relationship between two DNA or polypeptide sequences, simply means that they are functionally related to each other.
  • a presequence is operably linked to a peptide if it functions as a signal sequence, participating in the secretion of the mature form of the protein most probably involving cleavage of the signal sequence.
  • a promoter is operably linked to a coding sequence if it controls the transcription of the sequence; a ribosome binding site is operably linked to a coding sequence if it is positioned so as to permit translation.
  • TF tissue factor
  • FVIIa Factor VIIa
  • TFPI tissue factor pathway inhibitor
  • ATIII Antithrombin III
  • FXa Factor Xa
  • FXIa Factor XIa
  • FXIIa Factor XIIa
  • APPI Alzheimer's amyloid ⁇ -protein precursor inhibitor
  • TF 1-243 E.
  • coli derived recombinant human tissue factor encompassing residues 1-243; BPTI, basic pancreatic trypsin inhibitor; K i *, apparent equilibrium dissociation constant; CHAPS, 3- (3-cholamidopropyl)dimethylammonio!-1-propanesulfonate; PBS, phosphate buffered saline; BSA, bovine serum albumin; HPLC, high performance liquid chromatography; PT, prothrombin time; APTT, activated partial thromboplastin time.
  • Putative contact residues in the primary binding loop (residues 11-19) and secondary binding loop (residues 34, 38 and 39), (see FIG. 2) were altered by Kunkel mutagenesis as described in Example 1. Variants were then assayed for their ability to inhibit TF•FVIIa and several other serine proteases.
  • residues at other positions in the binding loop were Pro at position 11, Leu and Met at position 17, Met and Ile at position 18, and Leu or Lys at position 19.
  • inhibition of TF•FVIIa was also observed when residues Arg, Ala, Glu, Gly, or Thr at position 11, Ile, Arg, Tyr, or Ser at position 17, Leu, Tyr, His, or Phe at position 18, and Arg, Ala, or Ile at position 19 were incorporated into the Kunitz domain.
  • a number of residues were most preferable at position 34 including Val, Ile and Tyr.
  • Other residues here included Leu, Phe, Trp, and Ser.
  • the residues at positions 13 and 39 which are in close proximity to one another (Hynes, T. R.
  • inhibitors in FIG. 4 represent Kunitz domain inhibitors that are able to potently inhibit TF•FVIIa in the absence of FXa.
  • the TF7I-C variant differs by 4 key amino acids (Thr11Pro, Met17Leu, Ser19Leu and Gly39Tyr) compared to wild type APPI and results in an increase in affinity for the TF•FVIIa complex of greater than 150-fold.
  • the first Kunitz domain of TFPI itself does not potently inhibit TF•FVIIa, having a K i * of ca. 600 nM.
  • TF7I-C is much more effective than APPI at prolonging the clotting time in the APTT assay, a measure of the intrinsic coagulation pathway (FIG. 7). This is consistent with more potent inhibition of FXIa and kallikrein by TF7I-C compared to APPI.
  • thrombi and emboli Thrombosis in Cardiovascular Disorders, (Fuster, V. and Verstraete, M., eds.), W. B. Saunders, Philadelphia 1992!). These are a major cause of medical morbidity, leading to phlebitis, infarction, and stroke, and of mortality, from stroke and pulmonary and cardiac emboli. A large percentage of such patients have no antecedent risk factors, and develop venous thrombophlebitis and subsequent pulmonary emboli without a known cause. Other patients who form venous thrombi have underlying diseases known to predispose to these syndromes.
  • Some of these patients may have genetic or acquired deficiencies of factors that normally prevent hypercoagulability, such as antithrombin III. Others have mechanical obstructions to venous flow, such as tumor masses, that lead to low flow states and thrombosis. Patients with malignancy have a high incidence of thrombotic phenomena, for unclear reasons. Antithrombotic therapy in this situation with currently available agents is dangerous and often ineffective.
  • Atherosclerosis Patients with atherosclerosis are predisposed to arterial thromboembolic phenomena for a variety of reasons. Atherosclerotic plaques form niduses for platelet plugs and thrombi that lead to vascular narrowing and occlusion, resulting in myocardial and cerebral ischemic disease. Thrombi that break off and are released into the circulation can cause infarction of different organs, especially the brain, extremities, heart and kidneys. After myocardial infarctions, clots can form in weak, poorly functioning cardiac chambers and be released into the circulation to cause emboli. All such patients with atrial fibrillation are felt to be at great risk for stroke and require antithrombotic therapy.
  • thrombolytic therapy for acute myocardial infarction has become an established procedure for patients (Collen, D. and Stump, D., Ann Rev Med . 39:405-423 1988!).
  • currently available thrombolytic agents are not effective in all patients which is manifest by reocclusion, resistance to reperfusion, prolonged times to achieve normal coronary flow and the like.
  • a large category of patients including those with cancer, atherosclerosis, coronary artery disease (PTCA, CABG, Post MI, etc.), unstable angina, artificial heart valves, and a history of stroke, transient ischemic attacks, atrial fibrillation, deep vein thrombosis, phlebitis, or pulmonary emboli, are candidates for limited or chronic antithrombotic therapy.
  • this therapy is often ineffective or morbid in its own right. This is partially because the number of available therapeutic agents is limited.
  • Available antiplatelet agents such as aspirin, inhibit the cyclooxygenase-induced activation of platelets only and are often inadequate for therapy.
  • Available anticoagulants include heparin and warfarin which are not always efficacious and can often have side effects including increased bleeding risk and problems associated with monitoring these therapies.
  • An agent which effectively inhibits the formation of fibrin from fibrinogen should accordingly be particularly useful in therapeutic intervention in a large group of disorders characterized by a hypercoagulable state.
  • the compounds of the present invention may be utilized in compositions with a pharmaceutically acceptable excipient for injectible administration, in compounds such as tablets, capsules, or elixirs for oral administration.
  • Animals in need of treatment using compounds of the present invention can be administered dosages that will provide optimal efficacy.
  • the dose and method of administration will vary from animal to animal, and be dependent upon such factors as weight, diet, concurrent medication, and other factors which those skilled in the medical arts will recognize.
  • TF•FVIIa is an appropriate target for the intervention in coagulation processes because it is thought to initiate the cascade (see FIG. 1) (Broze Jr., G. J. et al., Biochemistry 29: 7539-7546 1990; Broze Jr., G. J., Semin. Hematol. 29: 159-169 1992!).
  • the inhibition of FVIIa, FXIa, and/or plasma kallikrein by agents described herein represents an approach for clinical intervention in various thrombotic disorders.
  • the agents described herein are useful in the treatment of thrombosis.
  • the instant inhibitors are especially useful as adjunct therapy for thrombolysis, unstable angina, deep vein thrombosis, hip replacement, coronary artery bypass graft, percutaneous transluminal coronary angioplasty, pulmonary embolism, septic shock, and DIC.
  • the agents described herein are also useful in the treatment of diseases where intervention in the activation of the contact pathway or neutrophil activation is indicated (e.g. inflammation, coagulation, fibrinolysis, and complement activation). More specifically, the instant inhibitors are especially useful in the treatment of diseases where inhibition of FXIa, kallikrein, FXIIa, FXa, and HLE, complement is indicated (see FIG. 1) as for example in the treatment of sepsis or septic shock, inflammation, ARDS, DIC, hypotension, cardiopulmonary bypass surgery, and for bleeding from postoperative surgery.
  • diseases where intervention in the activation of the contact pathway or neutrophil activation is indicated e.g. inflammation, coagulation, fibrinolysis, and complement activation.
  • the instant inhibitors are especially useful in the treatment of diseases where inhibition of FXIa, kallikrein, FXIIa, FXa, and HLE, complement is indicated (see FIG. 1) as for example in the treatment of sepsis or septic shock, inflammation,
  • the agents described herein may be useful in clinical situations that require acute or chronic therapy. It is anticipated that indications for which acute therapy is indicated are more preferred than those for chronic therapy.
  • the pharmaceutical use of foreign or mutant human proteins may be immunogenic; however foreign proteins are used to treat acute indications.
  • An example of such a protein is streptokinase, a protein derived from streptococci that acts as a fibrinolytic and is commonly used to treat acute myocardial infarction.
  • the agents described herein may elicit an immune response; however related foreign proteins such as BPTI have been used in humans clinically and are not anticipated to elicit a serious immune response.
  • PEG polyethylene glycol
  • One method of producing the Kunitz domain polypeptides of Formula I involves chemical synthesis of the protein, followed by treatment under oxidizing conditions appropriate to obtain the native conformation, that is, the correct disulfide bond linkages. This can be accomplished using methodologies well known to those skilled in the art (see Kelley, R. F. and Winkler, M. E. in Genetic Engineering Principles and Methods, (Setlow, J. K., ed.)., Plenum Press, New York, vol. 12, pp. 1-19 1990!; Stewart, J. M. and Young, J. D. Solid Phase Peptide Synthesis Pierce Chemical Co. Rockford, Ill. 1984!).
  • Polypeptides of the invention may be prepared using solid phase peptide synthesis (Merrifield, J. Am. Chem. Soc., 85:2149 1964!; Houghten, Proc. Natl. Acad. Sci. USA 82:5132 1985!).
  • Solid phase synthesis begins at the carboxy-terminus of the putative peptide by coupling a protected amino acid to a suitable resin, as shown in FIGS. 1-1 and 1-2, on pages 2 and 4 of Stewart and Young supra.
  • the carboxyl terminal amino acid with its ⁇ -amino group suitably protected, is coupled to a chloromethylated polystyrene resin (see FIG. 1-4, page 10 of Stewart and Young supra.).
  • a chloromethylated polystyrene resin see FIG. 1-4, page 10 of Stewart and Young supra.
  • TFA trifluoroacetic acid
  • ⁇ -amino- and, if necessary, side-chain-protected amino acids are then coupled sequentially in the desired order by condensation to obtain an intermediate compound connected to the resin.
  • some amino acids may be coupled to one another forming a peptide prior to addition of the peptide to the growing solid phase polypeptide chain.
  • the condensation between two amino acids, or an amino acid and a peptide, or a peptide and a peptide can be carried out according to the usual condensation methods such as azide method, mixed acid anhydride method, DCC (dicyclohexylcarbodiimide) method, active ester method (p-nitrophenyl ester method, BOP benzotriazole-1-yl-oxy-tris(dimethylamino)phosphonium hexafluorophosphate! method, N-hydroxysuccinic acid imido ester method, etc.), and Woodward reagent K method.
  • the peptide is attached to an insoluble carrier at the C-terminal amino acid.
  • halomethyl resin such as chloromethyl resin and bromomethyl resin, hydroxymethyl resin, aminomethyl resin, benzhydrylamine resin, and t-alkyloxycarbonyl-hydrazide resin can be used.
  • benzyloxycarbonyl (abbreviated Z), isonicotinyloxycarbonyl (iNOC), O-chlorobenzyloxycarbonyl Z(NO 2 !, p-methoxybenzyloxycarbonyl Z(OMe)!, t-butoxycarbonyl, (Boc), t-amyioxycarbonyl (Aoc), isobornyloxycarbonyl, adamatyloxycarbonyl, 2-(4-biphenyl)-2-propyloxycarbonyl (Bpoc), 9-fluorenylmethoxycarbonyl (Fmoc), methylsulfonyiethoxycarbonyl (Msc), trifluoroacetyl, phthalyl, formyl, 2-nitrophenylsulphenyl (NPS), diphenylphosphinothioyl (Pp
  • protective groups for carboxy group there can be exemplified, for example, benzyl ester (OBzl), cyclohexyl ester (Chx), 4-nitrobenzyl ester (ONb), t-butyl ester (Obut), 4-pyridylmethyl ester (OPic), and the like. It is desirable that specific amino acids such as arginine, cysteine, and serine possessing a functional group other than amino and carboxyl groups are protected by a suitable protective group as occasion demands.
  • the guanidino group in arginine may be protected with nitro, p-toluenesulfonyl, benzyloxycarbonyl, adamantyloxycarbonyl, p-methoxybenzenesulfonyl, 4-methoxy-2,6-dimethylbenzenesulfonyl (Mds), 1,3,5-trimethylphenysulfonyl (Mts), and the like.
  • the thiol group in cysteine may be protected with p-methoxybenzyl, triphenylmethyl, acetylaminomethyl ethylcarbamoyl, 4-methylbenzyl, 2,4,6-trimethy-benzyl (Tmb) etc, and the hydroxyl group in the serine can be protected with benzyl, t-butyl, acetyl, tetrahydropyranyl etc.
  • the intermediate peptide is removed from the resin support by treatment with a reagent, such as liquid HF and one or more thio-containing scavengers, which not only cleaves the peptide from the resin, but also cleaves all the remaining side-chain protecting groups.
  • a reagent such as liquid HF and one or more thio-containing scavengers, which not only cleaves the peptide from the resin, but also cleaves all the remaining side-chain protecting groups.
  • a reagent such as liquid HF and one or more thio-containing scavengers
  • a thio-cresol and cresol scavenger mixture is used.
  • the resin is washed with ether, and immediately transferred to a large volume of dilute acetic acid to solubilize and minimize intermolecular cross-linking.
  • a 250 ⁇ M polypeptide concentration is diluted in about 2 liters of 0.1M acetic acid solution. The solution is then stirred and its pH adjusted to about 8.0 using ammonium hydroxide. Upon pH adjustment, the polypeptide takes its desired conformational arrangement.
  • Kunitz domains can be made either by chemical synthesis, described above, or by semisynthesis. The chemical synthesis or semisynthesis methods of making allow the possibility of non-natural amino acid residues to be incorporated. This has been carried out for Kunitz domains and related proteins as previously described (Beckmann, J. et al., Eur. J. Biochem. 176: 675-682 1988!; Bigler, T. L. et al., Prot. Sci. 2: 786-799 1993!).
  • the purified protein may be produced using standard recombinant DNA techniques. These techniques contemplate, in simplified form, taking a gene encoding the Kunitz domain polypeptides of Formula I; inserting it into an appropriate vector; inserting the vector into an appropriate host cell; culturing the host cell to cause expression of the Kunitz domain polypeptides of Formula I; and purifying the protein produced thereby.
  • DNA sequence encoding the Kunitz domain polypeptides of Formula I is cloned and manipulated so that it may be expressed in a convenient host.
  • DNA encoding Formula I polypeptides can be obtained by synthetically constructing the DNA sequence (Sambrook, J. et al,, Molecular Cloning (2nd ed.), Cold Spring Harbor Laboratory, New York 1989!).
  • the DNA encoding Formula I peptides is then inserted into an appropriate plasmid or vector which is used to transform a host cell.
  • plasmid vectors containing replication and control sequences which are derived from species compatible with the host cell are used in connection with those hosts.
  • the vector ordinarily carries a replication site, as well as sequences which encode proteins that are capable of providing phenotypic selection in transformed cells.
  • E. coli may be transformed using pBR322, a plasmid derived from an E. coli species (Mandel, M. et al., J. Mol. Biol. 53:154 1970!).
  • Plasmid pBR322 contains genes for ampicillin and tetracycline resistance, and thus provides easy means for selection.
  • Other vectors include different features such as different promoters, which are often important in expression.
  • plasmids pKK223-3, pDR720, and pPL-lambda represent expression vectors with the tac, trp, or P L promoters that are currently available (Pharmacia Biotechnology).
  • a preferred vector is pSAlz1. This vector was created as described in Example 1 and contains origins of replication for E. coli, the alkaline phosphatase promoter, the stII signal sequence and APPI variant gene, and the ampicillin resistance gene.
  • Other preferred vectors are pBO475, pR1T5 and pR1T2T (Pharmacia Biotechnology). These vectors contain appropriate promoters followed by the Z domain of protein A, allowing genes inserted into the vectors to be expressed as fusion proteins. Further discussion of these vectors may be found below.
  • vectors can be constructed using standard techniques by combining the relevant traits of the vectors described herein.
  • Relevant traits of the vector include the promoter, the ribosome binding site, the APPI variant gene or gene fusion (the Z domain of protein A and APPI variant and its linker), the signal sequence, the antibiotic resistance markers, the copy number, and the appropriate origins of replication.
  • Kunitz domains have been expressed as intact secreted proteins (Castro, M. et al., FEBS Lett. 267: 207-212 1990!), intracellularly expressed proteins (Altman, J. D. et al., Protein Eng. 4: 593-600 1991!), or as fusion proteins (Sinha, S. et al., J. Biol. Chem. 266: 21011-21013 1991!; Lauritzen, C. et al., Prot. Express. Purif. 2: 372-378 1991!; Auerswald, E. A. et al., Biol. Chem. Hoppe-Seyler 369: 27-35 1988!).
  • the host cell may be prokaryotic or eukaryotic.
  • Prokaryotes are preferred for cloning and expressing DNA sequences to produce parent polypeptides, segment substituted polypeptides, residue-substituted polypeptides and polypeptide variants.
  • E. coli K12 strain 294 ATCC No. 31446
  • E. coli B E. coli X1776
  • E. coli c600 and c600hfl E. coli W3110 (F-, gamma-, prototrophic/ATCC No.
  • prokaryote E. coli W3110 (ATCC 27325).
  • the polypeptides When expressed by prokaryotes the polypeptides typically contain an N-terminal methionine or a formyl methionine and are not glycosylated. In the case of fusion proteins, the N-terminal methionine or formyl methionine resides on the amino terminus of the fusion protein or the signal sequence of the fusion protein.
  • eukaryotic organisms such as yeast cultures, or cells derived from multicellular organisms may be used.
  • any such cell culture is workable.
  • interest has been greatest in vertebrate cells, and propagation of vertebrate cells in culture (tissue culture) has become a reproducible procedure (Tissue Culture, Academic Press, Kruse and Patterson, eds. 1973!).
  • useful host cell lines are VERO and HeLa cells, Chinese Hamster Ovary (CHO) cell lines, W138, 293, BHK, COS-7 and MDCK cell lines.
  • Yeast expression systems have been used to make Kunitz domains (Wagner, S. L. et al., Biochem. Biophys. Res. Commun.
  • yeast Pichia pastoris has been used successfully using the Saccharomyces cerevisiae ⁇ mating factor prepro signal sequence and the P. pastoris alcohol oxidase AOX1 promoter and terminator sequences.
  • Other yeast expression vectors and hosts commonly used to express heterologous proteins are also contemplated.
  • a variation on the above procedures contemplates the use of gene fusions, wherein the gene encoding the APPI variant is associated, in the vector, with a gene encoding another protein or a fragment of another protein.
  • the "other" protein is often a protein or peptide which can be secreted by the cell, making it possible to isolate and purify the desired protein from the culture medium and eliminating the necessity of destroying the host cells which arises when the desired protein remains inside the cell.
  • the fusion protein can be expressed intracellularly. It is useful to use fusion proteins that are highly expressed.
  • APPI variants expressed as fusion proteins may be properly folded or may require folding to obtain the native structure.
  • the properly folded fusion protein may be active and useful as a serine protease incorrect. More preferred would be the correctly folded native protein that is obtained from the fusion protein by methods known in the art.
  • Fusion proteins can be cleaved using chemicals, such as cyanogen bromide, which cleaves at a methionine, or hydroxylamine, which cleaves between an Asn and Gly. Using standard recombinant DNA methodology, the nucleotide base pairs encoding these amino acids may be inserted just prior to the 5' end of the APPI variant gene.
  • proteolytic cleavage of fusion proteins which has been recently reviewed (Carter, P. in Protein Purification: From Molecular Mechanisms to Large-Scale Processes, (Ladisch, M. R., Willson, R. C., Painton, C. C., and Builder, S. E., eds.), American Chemical Society Symposium Series No. 427, Ch 13, pp. 181-193 1990!).
  • a peptide linker that is amenable to cleavage by the protease used is inserted between the "other" protein (e.g., the Z domain of protein A) and the protein of interest, such as an APPI variant.
  • the nucleotide base pairs encoding the linker are inserted between the genes or gene fragments coding for the other proteins.
  • Proteolytic cleavage of the partially purified fusion protein containing the correct linker can then be carried out on either the native fusion protein, or the reduced or denatured fusion protein.
  • the protein may or may not be properly folded when expressed as a fusion protein.
  • the specific peptide linker containing the cleavage site may or may not be accessible to the protease.
  • the protein When denaturing and refolding are needed, typically the protein is treated with a chaotrope, such a guanidine HCl, and is then treated with a redox buffer, containing, for example, reduced and oxidized dithiothreitol or glutathione at the appropriate ratios, pH, and temperature, such that the protein of interest is refolded to its native structure.
  • a chaotrope such as guanidine HCl
  • a redox buffer containing, for example, reduced and oxidized dithiothreitol or glutathione at the appropriate ratios, pH, and temperature, such that the protein of interest is refolded to its native structure.
  • mutant APPI DNA which encodes for additions, deletions, or changes in amino acid sequence of the resultant protein relative to the parent APPI molecule.
  • site specific mutagenesis (Kunkel et al., Methods Enzymol. 204:125-139 1991!; Carter, P., et al., Nucl. Acids. Res. 13:4331 1986!; Zoller, M. J. et al., Nucl. Acids Res. 10:6487 1982!), cassette mutagenesis (Wells, J. A., et al., Gene 34:315 1985!), restriction selection mutagenesis (Wells, J. A., et al., Philos. Trans, R. Soc. London SerA 317, 415 1986! or other known techniques may be performed on the APPI DNA.
  • mutant DNA can then be used in place of the parent DNA by insertion into the aforementioned expression vectors.
  • Growth of host bacteria containing the expression vectors with the mutant DNA allows the production of mutant APPI (i.e., analogs or homologs of APPI), which can be isolated as described herein.
  • APPI variants Purification and characterization of APPI variants may be carried out by any art standard technique including gel filtration, ion exchange, hydrophobic interaction, and affinity chromatography.
  • recombinant APPI variants were purified from the media of E. coli grown in 10 l fermentors or shake flasks by chromatography on a trypsin affinity column followed by reverse phase C18 HPLC.
  • variant proteins were expressed in and purified from E. coli.
  • the Kunitz domains were concentrated and partially purified from the media using a trypsin affinity column.
  • the final purification was carried out using reverse phase C18 HPLC as described in Example 2.
  • the expression level of most of the variants was ca. 1 mg/L in shake flasks and 80-100 mg/L in 10 L fermentations.
  • protein sequences were verified by mass spectrometry for the correct mass predicted from the sequence, assuming that all three disulfides were formed; all were within the error of this measurement ( ⁇ 2 amu).
  • HPLC chromatographs of inhibitors containing a Met commonly displayed a small peak eluting just before or just after the major inhibitor peak. This was a result of methionine oxidation to the sulfoxide.
  • K i * Apparent equilibrium dissociation constants (K i *) were determined using methods derived for tight-binding inhibitors (Bieth, J., Proteinase Inhibitors 463-469 1974!; Williams, J. W. and Morrison, J. F., Methods Enzymol 63: 437-467 1979!), assuming enzyme and inhibitor form a reversible complex with a 1:1 stoichiometry as has been observed for the interaction of Kunitz domains with serine proteases (Bode, W. and R. Huber, Eur. J. Biochem. 204: 433-451 1992; Laskowski, M., Jr. and I. Kato, Annu. Rev. Biochem. 49: 593-626 1980!).
  • Equation 1 The data were fit by nonlinear regression analysis to Equation 1: ##EQU1## where V i /V o is the fractional activity (steady-state inhibited rate divided by the uninhibited rate), E o ! is the total FVIIa active site concentration, and I o ! is the total inhibitor concentration. Variants were assayed for their binding affinity to TF•FVIIa and those with K i * values ranging from ca. 1-500 nM are shown in FIG. 4. The inhibition of TF•FVIIa by TF7I-C and APPI under equilibrium conditions is shown in FIG. 5; apparent K i * values of 1.9 ⁇ 0.4 nM and 301 ⁇ 44 nM were calculated for TF7I-C and APPI with TF•FVIIa, respectively (FIG. 4).
  • TF7I-C is also a potent inhibitor of FXIa and plasma kallikrein and a moderate inhibitor of plasmin (FIG. 4).
  • the K i * for FXa 90 nM and was >10 ⁇ M for activated protein C, thrombin, or FXIIa.
  • Other inhibitors were more specific inhibitors of TF•FVIIa with respect to FXIa, plasma kallikrein, or plasmin (FIG. 4).
  • both TF7I-C and APPI prolonged the clotting time in a concentration dependent manner (FIG. 6). This is consistent with the ability of these inhibitors to prevent FX activation through inhibition of the TF•FVIIa complex.
  • TF7I-C prolonged the clotting time 4-fold at ca. 20 ⁇ M, whereas the same concentration of APPI resulted in only a 1.5-fold increase in the clotting time.
  • TF7I-C also showed concentration dependent inhibition of the surface mediated contact activation pathway, as measured by the activated partial thromboplastin time assay (APTT) described in Example 4, a greater than 10-fold prolongation of the clotting time at ca. 7 ⁇ M was observed (FIG. 7).
  • APTT activated partial thromboplastin time assay
  • Dosage formulations of the compounds of the present invention to be used for therapeutic applications must be sterile. Sterility is readily accomplished by filtration through sterile filtration membranes such as 0.2 ⁇ membranes. Protein formulations ordinarily will be stored in lyophilized form or as an aqueous solution. The pH of the protein preparations typically will be between about 3 and 11, more preferably from about 5 to 9, and most preferably from about 7 to 8. The preferred route of administration is by hypodermic needle.
  • Therapeutic protein formulations are generally placed into a container having a sterile access port, for example, an intravenous solution bag or vial having a stopper pierceable by a hypodermic injection needle.
  • Therapeutically effective dosages may be determined by either in vitro (see assays above) or in vivo methods. Based upon such assay techniques, a therapeutically effective dosage range may be determined. The range of therapeutically effective dosages will naturally be affected by the route of administration. For injection by hypodermic needle, it may be assumed that the dosage is delivered into the body's fluids. For other routes of administration, the adsorption efficiency must be individually determined for APPI variants by methods well-known in pharmacology.
  • the range of therapeutic dosages may range from about 0.001 nM to about 1.0 mM, more preferably from about 0.1 nM to about 100 ⁇ M, and most preferably from about 1.0 nM to about 50 ⁇ M.
  • a typical formulation of APPI variants as a pharmaceutical composition contains from about 0.5 to 500 mg of a compound or mixture of compounds as either the free acid or base form or as a pharmaceutically acceptable salt. These compounds or mixtures are then compounded with a physiologically acceptable vehicle, carrier, excipient, binder, preservative, or stabilizer, etc., as called for by accepted pharmaceutical practice. The amount of active ingredient in these compositions is such that a suitable dosage in the range indicated is obtained.
  • Sterile compositions for injection can be formulated according to conventional pharmaceutical practice. For example, dissolution or suspension of the active compound in a vehicle such as water or naturally occurring vegetable oil like sesame, peanut, or cottonseed oil or a synthetic fatty vehicle like ethyl oleate or the like may be desired. Buffers, preservatives, antioxidants and the like can be incorporated according to accepted pharmaceutical practice.
  • Human Factor VIIa, Factor Xa, Factor XIa, activated protein C and thrombin were purchased from Haematologic Technologies Inc. (Essex Jct., Vt.). Human plasma kallikrein and Factor XIIa were purchased from Enzyme Research Laboratories, Inc. (South Bend, Ind.). Recombinant human tissue factor 1-243 (TF 1-243 ) was produced in E. coli and purified as previously described (Paborsky, L. R. et al., Biochemistry 28: 8072-8077 1989!; Paborsky, L. R. et al., J. Biol. Chem. 266: 21911-21916 1991!).
  • Bovine trypsin, 4-methylumbelliferyl p-guanidinobenzoate and CHAPS were purchased from Sigma Chemicals, Inc.
  • Bovine serum albumin (BSA) Fraction V was obtained from Calbiochem (La Jolla, Calif.).
  • N.sup. ⁇ -Benzoyl-L-arginine-p-nitroanilide was purchased from Bachem California (Torrance, Calif.).
  • Human plasmin, S-2302, S-2251 and S-2366 were purchased from Kabi Vitrum (Sweden) and Spectrozyme fXa was purchased from American Diagnostica (Greenwich, Conn.).
  • Affigel-10 was obtained from Bio-Rad Laboratories (Richmond, Calif.). All other reagents were obtained were of the highest grade commercially available.
  • the plasmid pSAlz1 was constructed by inserting a synthetic gene encoding the APPI sequence into an appropriate expression vector for secretion of APPI into the periplasm and media.
  • the pSAlz1 vector contained the alkaline phosphatase promoter, stII secretion signal, the APPI gene, the f1 and coE1 origins of replication, and the ampicillin resistance gene as described by Castro et al. (Castro, M. et al., FEBS Lett. 267: 207-212 1990!).
  • the construction of APPI mutants using the pSAlz1 vector was accomplished using site-directed oligonucleotide mutagenesis in as previously described (Kunkel, T. A.
  • Phagemids encoding either APPI or the selected mutants were transformed into E. coli strain 27C7, a derivative of E. coli W3110, for expression of the Kunitz domain inhibitors. Overnight saturated cultures were inoculated (1%) into 250 ml of low phosphate minimal media (Chang, C. N. et al., Gene 55: 189-196 1987! containing 50 ⁇ g/ml ampicillin and grown for 20 h at 37° C. Inhibitors were secreted into the periplasm by virtue of the stIl signal sequence and eventually leaked into the media.
  • Enzyme inhibition assays were conducted in a microtiter format and absorbance changes were monitored on an SLT EAR340AT plate reader controlled by a Macintosh SE computer equipped with Biometallics DeltaSoftlI software. Nonlinear regression analysis was carried out using KaleidaGraph v3.01 (Synergy Software).
  • Inhibitor stocks were diluted in the range of 5-2000 nM; concentrations were accurately determined by titration with trypsin that had been active site-titrated using 4-methylumbelliferyl p-guanidinobenzoate (Jameson, G. W. et al., Biochem. J. 131: 107-117 1973!).
  • the proteases tested were FVIIa (10 nM, Buffer A, 0.7 mM S2366), FXIa (1.0 nM, Buffer B containing 1 mg/ml BSA, 0.7 mM S2366), plasma kallikrein (3.5 nM, Buffer B, 0.5 mM S2302), and plasmin (15 nM, Buffer B, 1 mM S2251).
  • Buffer A contains 50 mM Tris, pH 7.5, 100 mM NaCl, 10 mM CaCl 2 , 0.5% BSA, 60 nM TF- 1-243 , and 1 mM CHAPS (Sigma).
  • Buffer B contains 50 mM Tris, pH 7.5, 100 mM NaCl, 2 mM CaCl 2 and 0.005% Triton X-100.
  • Clotting times were performed using the ACL 300 Research Coagulation Analyzer.
  • the incubation time was set at 120 sec and acquisition time at 120 to 600 sec depending on the expected outcome of the assay.
  • Membranes from 293 cells expressing full length TF (Paborsky, L. R. et al., Biochemistry 28: 8072-8077 1989!) were premixed with CaCl 2 .
  • the sample (plasma and inhibitor) and reagent (CaCl 2 /TF) were automatically mixed together after a 2 min incubation at 37° C.
  • the clotting time was determined by optical assessment.
  • the total incubation time of inhibitor with plasma before addition of CaCl 2 /TF was ca. 5 min. Final concentrations were 2 to 20 ⁇ M inhibitor, 3.7 nM TF (0.9 ⁇ g/ml by protein content), 22.5 mM CaCl 2 , and 50% plasma in a total volume of 160 ⁇ L.
  • the activation time was set at 120 sec and acquisition time at 300 to 600 sec depending on the expected outcome of the assay. Citrated normal human plasma and inhibitor were incubated together. The sample (plasma and inhibitor) and activator (Instrumentation Laboratories Ellagic acid/Phospholipid mix Test Reagent) were automatically pipetted and incubated together for 2 min at 37° C., then CaCl 2 was added and clotting time determined by means of optical assessment. The total incubation time of inhibitor with plasma was ca. 3 min before addition of activator, and 5 min before addition of CaCl 2 .

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US08/206,310 US5795954A (en) 1994-03-04 1994-03-04 Factor VIIa inhibitors from Kunitz domain proteins
US08/398,010 US5834244A (en) 1994-03-04 1995-03-03 Factor VIIa inhibitors from Kunitz domain proteins
PCT/US1995/002637 WO1995023860A2 (fr) 1994-03-04 1995-03-03 PROTEINES INHIBITRICES PROPRES AU DOMAINE DE KÜNITZ DERIVEES DE L'INHIBITEUR DU PRECURSEUR DE LA β-PROTEINE AMYLOIDE DE LA MALADIE D'ALZHEIMER
JP7523045A JPH09509838A (ja) 1994-03-04 1995-03-03 クニッツドメイン拮抗剤蛋白質
US08/399,115 US5880256A (en) 1994-03-04 1995-03-03 Factor VIIa inhibitors from Kunitz domain proteins
MX9603775A MX9603775A (es) 1994-03-04 1995-03-03 Proteinas inhibidoras del dominio de kunitz, derivadas del inhibidor del precursor de la beta-proteina amiloide de alzheimer.
EP95913532A EP0748380A1 (fr) 1994-03-04 1995-03-03 PROTEINES INHIBITRICES PROPRES AU DOMAINE DE KÜNITZ DERIVEES DE L'INHIBITEUR DU PRECURSEUR DE LA $g(b)-PROTEINE AMYLOIDE DE LA MALADIE D'ALZHEIMER
CA002184058A CA2184058A1 (fr) 1994-03-04 1995-03-03 Proteines inhibitrices propres au domaine de kunitz derivees de l'inhibiteur du precurseur de la .beta.-proteine amyloide de la maladie d'alzheimer
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